Effects of canagliflozin on serum potassium in people with diabetes and chronic kidney disease: the CREDENCE trial

Eur Heart JPublished Post hoc analysis of the CREDENCE randomised trial

Primary result · Investigator-reported hyperkalaemia or initiation of potassium bindersResult — go to the resultHazard ratio 0.78 95% CI 0.64–0.95

Authors' conclusion

Among patients treated with renin-angiotensin-aldosterone system inhibitors, SGLT2 inhibition with canagliflozin may reduce the risk of hyperkalaemia in people with T2DM and CKD without increasing the risk of hypokalaemia.

Study context

Population
Participants with T2DM and chronic kidney disease (CKD) (99.9% on renin-angiotensin system blockade)
Participants
4,401 participants
Comparison
Canagliflozin vs placebo
Primary endpoint
Time to investigator-reported hyperkalaemia or initiation of potassium binders
Methodological detailsplacebo-controlled
  • Placebo-controlled

Primary result

As reported in the abstract

Investigator-reported hyperkalaemia or initiation of potassium binders

Hazard ratio

0.78

95% CI 0.64–0.95

P = 0.014

By group

Canagliflozin vs Placebo
HR 0.78 (95% CI 0.64–0.95); P = 0.014

Further findings

OutcomeHR (95% CI)P value
Laboratory-determined hyperkalaemia (serum potassium ≥6.0 mmol/L)0.77 (0.61–0.98)P = 0.031

Mean serum potassium over time

Mean serum potassium over time similar with canagliflozin and placebo

Safety

OutcomeHR (95% CI)P value
Laboratory-determined hypokalaemia (serum potassium <3.5 mmol/L)0.92 (0.71–1.20)P = 0.53

Original publication

Effects of canagliflozin on serum potassium in people with diabetes and chronic kidney disease: the CREDENCE trial. Eur Heart J. Published 23 August 2021. doi:10.1093/eurheartj/ehab497

Summarised from the published abstract; every number is checked against it

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